Celsr1 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Celsr1
cadherin, EGF LAG seven-pass G-type receptor 1
MGI:1100883

11 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Celsr1^Crsh/Celsr1⁺ Vangl2^Lp/Vangl2⁺ C3H.Cg-Vangl2^Lp Celsr1^Crsh	abnormal eyelid morphology	J:216413
	abnormal left-right axis patterning	J:216413
	craniorachischisis	J:216413
	omphalocele	J:216413
Celsr1^Crsh/Celsr1⁺ Vangl2^Lp/Vangl2⁺ involves: 101/H * BALB/c * C3H/HeH * CBA * LPT/Le	craniorachischisis	J:216413
	curly tail	J:216413
Celsr1^Crsh/Celsr1⁺ Scrib^Crc/Scrib⁺ C3H.Cg-Scrib^Crc Celsr1^Crsh	abnormal abdominal wall morphology	J:216413
	abnormal developmental patterning	J:216413
	abnormal eyelid development	J:216413
	abnormal eyelid morphology	J:216413
	craniorachischisis	J:216413
	curly tail	J:216413
	exencephaly	J:216413
	spina bifida	J:216413
Celsr1^Crsh/Celsr1⁺ Scrib^Crc/Scrib⁺ involves: 101/H * BALB/c * C3H/HeH * C57BL/6 * NMRI	craniorachischisis	J:216413
Celsr1^Crsh/Celsr1⁺ Scrib^Crc/Scrib⁺ Vangl2^Lp/Vangl2⁺ C3H.Cg-Vangl2^Lp Scrib^Crc Celsr1^Crsh	abnormal tail morphology	J:216413
	craniorachischisis	J:216413
	exencephaly	J:216413
Celsr1^Crsh/Celsr1⁺ Ptk7^chz/Ptk7⁺ involves: 101/H * BALB/c * BALB/cAnN * C3H/HeH	spina bifida	J:163834
Celsr1^Scy/Celsr1⁺ Scrib^Crc/Scrib⁺ C3H.Cg-Scrib^Crc Celsr1^Scy	abnormal abdominal wall morphology	J:216413
	abnormal eyelid morphology	J:216413
	craniorachischisis	J:216413

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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